A non-targeted LC-MS metabolic profiling of pregnancy: longitudinal evidence from healthy and pre-eclamptic pregnancies

dc.contributor.authorJääskeläinen Tiina
dc.contributor.authorKärkkäinen Olli
dc.contributor.authorJokkala Jenna
dc.contributor.authorKlåvus Anton
dc.contributor.authorHeinonen Seppo
dc.contributor.authorAuriola Seppo
dc.contributor.authorLehtonen Marko
dc.contributor.authorThe FINNPEC Core Investigator Group
dc.contributor.authorHanhineva Kati
dc.contributor.authorLaivuori Hannele
dc.contributor.organizationfi=elintarviketieteet|en=Food Sciences|
dc.contributor.organization-code1.2.246.10.2458963.20.15178954341
dc.converis.publication-id52300362
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/52300362
dc.date.accessioned2022-10-27T11:55:14Z
dc.date.available2022-10-27T11:55:14Z
dc.description.abstract<p>Introduction<br>Maternal metabolism changes substantially during pregnancy. However, few studies have used metabolomics technologies to characterize changes across gestation.<br>Objectives and methods<br>We applied liquid chromatography–mass spectrometry (LC–MS) based non-targeted metabolomics to determine whether the metabolic profile of serum differs throughout the pregnancy between pre-eclamptic and healthy women in the FINNPEC (Finnish Genetics of Preeclampsia Consortium) Study. Serum samples were available from early and late pregnancy.<br>Results<br>Progression of pregnancy had large-scale effects to the serum metabolite profile. Altogether 50 identified metabolites increased and 49 metabolites decreased when samples of early pregnancy were compared to samples of late pregnancy. The metabolic signatures of pregnancy were largely shared in pre-eclamptic and healthy women, only urea, monoacylglyceride 18:1 and glycerophosphocholine were identified to be increased in the pre-eclamptic women when compared to healthy controls.<br>Conclusions<br>Our study highlights the need of large-scale longitudinal metabolomic studies in non-complicated pregnancies before more detailed understanding of metabolism in adverse outcomes could be provided. Our findings are one of the first steps for a broader metabolic understanding of the physiological changes caused by pregnancy per se.<br></p>
dc.identifier.eissn1573-3890
dc.identifier.jour-issn1573-3882
dc.identifier.olddbid172818
dc.identifier.oldhandle10024/155912
dc.identifier.urihttps://www.utupub.fi/handle/11111/30653
dc.identifier.urlhttps://doi.org/10.1007/s11306-020-01752-5
dc.identifier.urnURN:NBN:fi-fe2022020818024
dc.language.isoen
dc.okm.affiliatedauthorHanhineva, Kati
dc.okm.discipline1182 Biochemistry, cell and molecular biologyen_GB
dc.okm.discipline3123 Gynaecology and paediatricsen_GB
dc.okm.discipline1182 Biokemia, solu- ja molekyylibiologiafi_FI
dc.okm.discipline3123 Naisten- ja lastentauditfi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherSpringer
dc.publisher.countryNetherlandsen_GB
dc.publisher.countryAlankomaatfi_FI
dc.publisher.country-codeNL
dc.relation.articlenumber20
dc.relation.doi10.1007/s11306-020-01752-5
dc.relation.ispartofjournalMetabolomics
dc.relation.volume17
dc.source.identifierhttps://www.utupub.fi/handle/10024/155912
dc.titleA non-targeted LC-MS metabolic profiling of pregnancy: longitudinal evidence from healthy and pre-eclamptic pregnancies
dc.year.issued2021

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